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Cited by 1,579

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

14-3-3 Proteins: Structure, Function, and Regulation

Fu, Haian, Subramanian, Romesh R., Masters, Shane C.·2000·Annual Review of Pharmacology and Toxicology

Abstract

The 14-3-3 proteins are a family of conserved regulatory molecules expressed in all eukaryotic cells. A striking feature of the 14-3-3 proteins is their ability to bind a multitude of functionally diverse signaling proteins, including kinases, phosphatases, and transmembrane receptors. This plethora of interacting proteins allows 14-3-3 to play important roles in a wide range of vital regulatory processes, such as mitogenic signal transduction, apoptotic cell death, and cell cycle control. In this review, we examine the structural basis for 14-3-3–ligand interactions, proposed functions of 14-3-3 in various signaling pathways, and emerging views of mechanisms that regulate 14-3-3 actions.

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Crossref · 10.1146/annurev.pharmtox.40.1.617

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Metadata

Authors
Fu, H., Subramanian, R. R., & Masters, S. C.
Venue
Annual Review of Pharmacology and Toxicology
Published
2000-04
Volume
40
Issue
1
Pages
617-647
ISSN
  • 0362-1642 (ISSN-L)
  • 1545-4304
OpenAlex
W2122772601
Cited by
1,579
References
3
FWCI
4.99
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: 14-3-3 Proteins: Structure, Function, and Regulation. https://app.cochat.ai/papers/10.1146/annurev.pharmtox.40.1.617
The paper
Fu, H., Subramanian, R. R., & Masters, S. C. (2000). 14-3-3 Proteins: Structure, Function, and Regulation. Annual Review of Pharmacology and Toxicology. https://doi.org/10.1146/annurev.pharmtox.40.1.617

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.